Loading...
Derniers dépôts
Nombre de documents
777
Nombre de notices
1 376
widget_cloud
Exercise
Myogenesis
Myositis
Heart
Nuclear envelope
Rare neuromuscular diseases
Dilated cardiomyopathy
Mouse model
CTG repeat contractions
Myotonic dystrophy type 1
Cytoskeleton
DMD
Myoblasts
Laminopathie
Myotonic Dystrophy type 1
Humans
Dermatomyositis
Actin
Centronuclear myopathy
Astrocyte
Clinical trials
Myasthenia gravis
Neuromuscular diseases
Aging
OPMD
Transgenic mouse model
Therapy
Calcium
Muscular dystrophy
Autoimmune diseases
Myopathy
Becker muscular dystrophy
Myotonic dystrophy
Congenital muscular dystrophy
Diagnosis
ALS
Satellite cell
Myasthenia Gravis MG
Errance diagnostique
Lamin A/C LMNA gene
Cell therapy
Treatment
LMNA gene
Heart failure
Genotype phenotype correlation
Dystrophin
Fabry disease
Autophagy
Satellite cells
Male
Muscle regeneration
AAV
FSHD
Congenital myopathy
Aged
RNA interference
Muscle
Cytokines
Cancer
Laminopathy
Myopathies
Mechanotransduction
Neuromuscular disease
Alternative splicing
Motoneuron
Transcriptomics
Myotonic Dystrophy
Trinucleotide repeat expansion
Cardiomyopathy
Autoantibodies
PABPN1
Autoimmunity
Neuromuscular junction
CMS
Skeletal muscle
Biomarkers
Outcome measures
Thérapie génique
COVID-19
Long read sequencing
Animals
Duchenne muscular dystrophy
Rare diseases
LMNA
Gene therapy
RNA biology
Dynamin 2
Regeneration
Inflammation
Biomarker
Laminopathies
Brain
Glutamate
CRISPRi
Fibrosis
Thymus
MBNL
Amyotrophic lateral sclerosis
Antisense oligonucleotides
Lamin A/C